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      The role of curing temperature and reactive aluminum species on characteristics of phosphate geopolymer

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      RSC Advances
      The Royal Society of Chemistry

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          Abstract

          The reaction of an acid phosphate with ferro/aluminosilicate materials is a slow-setting process at room temperature that requires several days to harden. Thus, various setting accelerators are generally used to achieve quick setting and demolding in a short period. This work aims to evaluate the benefits of phosphoric acid-containing soluble aluminum and heat curing on accelerating the reaction kinetic and strength development of phosphate geopolymers. The diluted phosphoric acid (PA, 50 wt%) and acid aluminum phosphate (PA, 50 wt%, Al/P = 1/3) solutions were prepared to activate volcanic ash, and the samples were cured at 20, 40, and 60 °C to produce the phosphate geopolymer binder. The phosphate geopolymer's reaction kinetics, mechanical properties, mineralogy, and microstructure were evaluated. The results revealed that when volcanic ash was activated with diluted phosphoric acid, the reaction mechanism that prevailed was the dissolution–enhancement–precipitation–condensation, and was also fostered when the heat curing was applied. While for the acid aluminum phosphate-activated volcanic ash, the mechanism is dissolution–inhibition–precipitation–condensation. That difference in reaction mechanism led to a higher compressive strength improvement at an early age (1 d, 3 d) for room temperature cured acid aluminum phosphate activated volcanic ash. In contrast, phosphoric acid-activated volcanic ash phosphate geopolymer developed a higher compressive strength at a late age (28 d). Moreover, heat curing is the most crucial parameter having a beneficial effect on compressive strength development as compared to acid aluminum phosphate activating solution.

          Abstract

          The diluted phosphoric acid and mild curing temperature foster the dissolution–enhancement–precipitation–condensation mechanism. While the dissolution–inhibition–precipitation–condensation mechanism occurs in the presence of any setting accelerator.

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          Chemically Bonded Phosphate Ceramics Twenty-First Century Materials with Diverse Applications

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            Chemically Bonded Phosphate Ceramics

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              Developments in Strategie Materials and Computational Design II Developments in Strategie Materials and Computational Design II

              A. N. WAGH (2011)
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                Author and article information

                Journal
                RSC Adv
                RSC Adv
                RA
                RSCACL
                RSC Advances
                The Royal Society of Chemistry
                2046-2069
                17 October 2022
                17 October 2022
                17 October 2022
                : 12
                : 46
                : 29653-29665
                Affiliations
                [a] Local Material Promotion Authority (MIPROMALO), MINRESI 2396, Nkolbikok Yaoundé Cameroon noel.djobo@ 123456mipromalo.cm/ noeldjobo@ 123456gmail.com +237 676597699 +237 676597699
                [b] Building Materials and Construction Chemistry, Technische Universität Berlin Gustav-Meyer-Allee 25 13355 Berlin Germany
                Author information
                https://orcid.org/0000-0002-2243-4841
                Article
                d2ra04562a
                10.1039/d2ra04562a
                9575157
                36321086
                8638c9f1-3ce6-4ba0-9f39-d03dfb26c8e1
                This journal is © The Royal Society of Chemistry
                History
                : 22 July 2022
                : 10 October 2022
                Page count
                Pages: 13
                Funding
                Funded by: Alexander von Humboldt-Stiftung, doi 10.13039/100005156;
                Award ID: CM-1201499-GF-P
                Categories
                Chemistry
                Custom metadata
                Paginated Article

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